ethyl 2-(1-(tert-butoxycarbonyl)piperidin-3-yl)thiazole-4-carboxylate

Base Information

Chemical Name:ethyl 2-(1-(tert-butoxycarbonyl)piperidin-3-yl)thiazole-4-carboxylate
CAS No.:1192248-02-4
Molecular Formula:C₁₆H₂₄N₂O₄S
Molecular Weight:340.444
Hs Code.:
Mol file:1192248-02-4.mol

Synonyms:tert-Butyl 3-[4-(ethoxycarbonyl)-1,3-thiazol-2-yl]piperidine-1-carboxylate

Suppliers and Price of ethyl 2-(1-(tert-butoxycarbonyl)piperidin-3-yl)thiazole-4-carboxylate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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American Custom Chemicals Corporation
ETHYL 2-(1-(TERT-BUTOXYCARBONYL)PIPERIDIN-3-YL)THIAZOLE-4-CARBOXYLATE 95.00%
5MG
$ 498.17

Total 0 raw suppliers

Chemical Property of ethyl 2-(1-(tert-butoxycarbonyl)piperidin-3-yl)thiazole-4-carboxylate

Chemical Property:

Purity/Quality:: ETHYL 2-(1-(TERT-BUTOXYCARBONYL)PIPERIDIN-3-YL)THIAZOLE-4-CARBOXYLATE 95.00% ^*data from reagent suppliers

Safty Information:

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Technology Process of ethyl 2-(1-(tert-butoxycarbonyl)piperidin-3-yl)thiazole-4-carboxylate

There total 4 articles about ethyl 2-(1-(tert-butoxycarbonyl)piperidin-3-yl)thiazole-4-carboxylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 50.0%

: 70-23-5
ethyl Bromopyruvate

: 274682-80-3
3-thiocarbamoylpiperidine-1-carboxylic acid tert-butyl ester

: 1192248-02-4
tert-Butyl 3-[4-(ethoxycarbonyl)-1,3-thiazol-2-yl]piperidine-1-carboxylate

Guidance literature:: With sodium iodide; In acetone; at 50 ℃; for 2h;

Reference yield:

: 4138-26-5,168749-30-2
nipecotamide

: 1192248-02-4
tert-Butyl 3-[4-(ethoxycarbonyl)-1,3-thiazol-2-yl]piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: chloroform / 20 °C

2: tetraphosphorus decasulfide; sodium carbonate / tetrahydrofuran / 1.5 h / 20 °C / Inert atmosphere

3: sodium iodide / acetone / 2 h / 50 °C

With tetraphosphorus decasulfide; sodium carbonate; sodium iodide; In tetrahydrofuran; chloroform; acetone;

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 1192248-02-4
tert-Butyl 3-[4-(ethoxycarbonyl)-1,3-thiazol-2-yl]piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: chloroform / 20 °C

2: tetraphosphorus decasulfide; sodium carbonate / tetrahydrofuran / 1.5 h / 20 °C / Inert atmosphere

3: sodium iodide / acetone / 2 h / 50 °C

With tetraphosphorus decasulfide; sodium carbonate; sodium iodide; In tetrahydrofuran; chloroform; acetone;